Evidence map›Paper›PMID 28403142›Full record

ArticlePloS one2017

Melatonin protects rats from radiotherapy-induced small intestine toxicity.

Beatriz Fernández-Gil, Ahmed E Abdel Moneim, Francisco Ortiz, Ying-Qiang Shen, Viviana Soto-Mercado, Miguel Mendivil-Perez, Ana Guerra-Librero, Darío Acuña-Castroviejo, María M Molina-Navarro, José M García-Verdugo and 5 more

Abstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

54 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Radiomitigators: Breakthroughs in Post-Radiation Recovery.Antioxidants (Basel, Switzerland) · 2026
    Review
  4. Article
  5. Review
  6. Review
  7. Dynamic change of gut microbiota in head and neck concurrent chemoradiotherapy patients and its potential value in the prediction of acute oral mucositis grade as well as quality of life.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
    Article
  8. Review
  9. Review
  10. Review
  11. Involvement of the SIRT1-NLRP3 pathway in the inflammatory response.Cell communication and signaling : CCS · 2023
    Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Standardized fraction of Xylocarpus moluccensis inhibits inflammation by modulating MAPK-NFκB and ROS-HIF1α-PKM2 activation.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2022
    Article
  18. Review
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Beatriz Fernández-GilInstituto de Biotecnología, Centro de Investigación Biomédica, Universidad de Granada, Granada, Spain.
Ahmed E Abdel MoneimDepartment of Zoology and Entomology, Faculty of Science, Helwan University, Cairo, Egypt.
Francisco OrtizInstituto de Biotecnología, Centro de Investigación Biomédica, Universidad de Granada, Granada, Spain.
Ying-Qiang ShenInstituto de Biotecnología, Centro de Investigación Biomédica, Universidad de Granada, Granada, Spain.
Viviana Soto-MercadoNeuroscience Research Group, Medical Research Institute, Faculty of Medicine, University of Antioquia, Medellin, Colombia.
Miguel Mendivil-PerezNeuroscience Research Group, Medical Research Institute, Faculty of Medicine, University of Antioquia, Medellin, Colombia.
Ana Guerra-LibreroInstituto de Biotecnología, Centro de Investigación Biomédica, Universidad de Granada, Granada, Spain.
Darío Acuña-CastroviejoInstituto de Biotecnología, Centro de Investigación Biomédica, Universidad de Granada, Granada, Spain.
María M Molina-NavarroInstituto Cavanilles, Universidad de Valencia, Valencia, Spain.
José M García-VerdugoInstituto Cavanilles, Universidad de Valencia, Valencia, Spain.
Ramy K A SayedDepartment of Anatomy and Embryology, Faculty of Veterinary Medicine, Sohag University, Sohag, Egypt.
Javier FloridoInstituto de Biotecnología, Centro de Investigación Biomédica, Universidad de Granada, Granada, Spain.
Juan D LunaDepartamento de Bioestadística, Facultad de Medicina, Universidad de Granada, Granada, Spain.
Luis Carlos LópezInstituto de Biotecnología, Centro de Investigación Biomédica, Universidad de Granada, Granada, Spain.
Germaine EscamesInstituto de Biotecnología, Centro de Investigación Biomédica, Universidad de Granada, Granada, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Radiotherapy-induced gut toxicity is among the most prevalent dose-limiting toxicities following radiotherapy. Prevention of radiation enteropathy requires protection of the small intestine. However, despite the prevalence and burden of this pathology, there are currently no effective treatments for radiotherapy-induced gut toxicity, and this pathology remains unclear. The present study aimed to investigate the changes induced in the rat small intestine after external irradiation of the tongue, and to explore the potential radio-protective effects of melatonin gel. Male Wistar rats were subjected to irradiation of their tongues with an X-Ray YXLON Y.Tu 320-D03 irradiator, receiving a dose of 7.5 Gy/day for 5 days. For 21 days post-irradiation, rats were treated with 45 mg/day melatonin gel or vehicle, by local application into their mouths. Our results showed that mitochondrial oxidative stress, bioenergetic impairment, and subsequent NLRP3 inflammasome activation were involved in the development of radiotherapy-induced gut toxicity. Oral treatment with melatonin gel had a protective effect in the small intestine, which was associated with mitochondrial protection and, consequently, with a reduced inflammatory response, blunting the NF-κB/NLRP3 inflammasome signaling activation. Thus, rats treated with melatonin gel showed reduced intestinal apoptosis, relieving mucosal dysfunction and facilitating intestinal mucosa recovery. Our findings suggest that oral treatment with melatonin gel may be a potential preventive therapy for radiotherapy-induced gut toxicity in cancer patients.

Indexed as

AnimalsApoptosisDrug Evaluation, PreclinicalGelsIntestinal MucosaIntestine, SmallMaleMelatoninNF-kappa BNLR Family, Pyrin Domain-Containing 3 ProteinOxidative PhosphorylationOxidative StressRadiation Injuries, ExperimentalRadiation-Protective AgentsRats, WistarTongueGelsMelatoninNF-kappa BNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, ratRadiation-Protective Agents

Identifiers

PMID28403142
PMCPMC5389624

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.